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The European Medicines Agency (EMA) is the EU agency responsible for evaluating and supervising medicines for human and veterinary use. Find information on medicines, news, events, FAQs and more on its homepage.
- Frequently Asked Questions
In the European Union (EU), herbal medicines are authorised...
- Medicines
The European Medicines Agency (EMA) facilitates development...
- About us
The European Medicines Agency (EMA) is a decentralised...
- Who We Are
The European Medicines Agency (EMA) is a decentralised...
- Frequently Asked Questions
La EMA es la agencia descentralizada que evalúa y supervisa la seguridad de los medicamentos en la UE y el EEE. Conoce sus funciones, cometidos, beneficios y contacto en su web oficial.
The EMA evaluates and monitors medicines for humans and animals in the EU and the EEA. It issues marketing authorisations, provides safety information, and supports research and development of new medicines.
The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).